DIVAS: a centralized genetic variant repository representing 150 000 individuals from multiple disease cohorts

Motivation: A plethora of sequenced and genotyped disease cohorts is available to the biomedical research community, spread across many portals and represented in various formats. Results: We have gathered several large studies, including GERA and GRU, and computed population- and disease-specific g...

Descripción completa

Detalles Bibliográficos
Autores principales: Cheng, Wei-Yi, Hakenberg, Jörg, Li, Shuyu Dan, Chen, Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Applications Notes
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681987/
https://www.ncbi.nlm.nih.gov/pubmed/26363178
http://dx.doi.org/10.1093/bioinformatics/btv511

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681987/
https://www.ncbi.nlm.nih.gov/pubmed/26363178
http://dx.doi.org/10.1093/bioinformatics/btv511

Ejemplares similares